Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion description "[X-linked lissencephaly with abnormal genitalia (XLAG) is a rare disorder caused by mutations in the aristaless-related homeobox (ARX) gene, located on Xp22.13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion evidence source_evidence_literature NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion SIO_000772 18458920 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion wasDerivedFrom befree-20150227 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion wasGeneratedBy ECO_0000203 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.